Canonical Allele Identifier: CA2659222608
Gene: USP34 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61378243dup , CM000664.2:g.61378243dup GRCh38
NC_000002.11:g.61605378dup , CM000664.1:g.61605378dup GRCh37
NC_000002.10:g.61458882dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000398571.7:c.1076+120dup MANE Select ENSP00000381577.2:n.1076+120dup
ENST00000398571.6:c.1076+120dup ENSP00000381577.2:n.1076+120dup
ENST00000453133.1:c.602+120dup
NM_014709.3:c.1076+120dup NP_055524.3:n.1076+120dup
NM_014709.4:c.1076+120dup MANE Select NP_055524.3:n.1076+120dup